rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Advances in genetics
    part number: Volume 63
    part name: Ion channel diseases
  title info:
    title: Ion channel diseases
  name:
    name part: Rouleau, Guy.
  name:
    name part: Gaspar, Claudia
    name part: Ph. D
  name:
    name part: ScienceDirect (Online service)
  type of resource: text
  genre: bibliography
  genre: Electronic books.
  origin info:
    place:
      place term: ne
    place:
      place term: Amsterdam
    place:
      place term: Boston
    publisher: Academic Press
    date issued: ©2008
    date issued: 2008
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: remote
    extent: 1 online resource (x, 157 pages) : illustrations.
  abstract: Ion channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic component. This volume presents a broad and comprehensive overview of the inherited channelopathies in humans, including clinical, genetic and molecular aspects of these conditions, as well as novel genomic and modeling research approaches. Also included is a review of potential therapeutic approaches for each of these conditions.
  table of contents: Front Cover; Ion Channel Diseases; Copyright Page; Contents; Contributors; Part I: Muscle Channelopathies; Chapter 1: Periodic Paralysis; I. Introduction; III. Hyperkalemic Periodic Paralysis; IV. Other Types of Periodic Paralysis; VI. Treatment and Care of hypoPP Patients; VII. Conclusion; Acknowledgments; I. Introduction; V. Myotonia Congenita in Animal Models; Acknowledgments; References; Chapter 3: Familial Hemiplegic Migraine; II. The Migraine Attack: Clinical Phases and Pathophysiology; III. The Migraine Aura and Cortical Spreading Depression; IV. Migraine as a Genetic Disorder
  table of contents: VI. Functional Consequences of FHM MutationsVIII. Concluding Remarks; Acknowledgments; Acknowledgments; Part II: Internal Diseases; Chapter 5: Channelopathies of Transepithelial Transport and Vesicular Function; I. Introduction; II. Disorders; III. Concluding Remarks; References; Index
  note: edited by Guy Rouleau, Claudia Gaspar.
  note: Includes bibliographical references and index.
  note: English.
  subject:
    topic: Ion channels
  subject:
    topic: Membrane disorders
  subject:
    topic: Ion Channels
  subject:
    topic: Canaux ioniques
  subject:
    topic: Membranes (Biologie)
    topic: Maladies
  subject:
    topic: Ion channels
  subject:
    topic: Membrane disorders
  classification: QH431.A1 A363 2008eb
  classification: 571.6/4
  related item:
    title info:
      title: Advances in genetics ; v. 63
  identifier: 9780123745279
  identifier: 0123745276
  identifier: 1282287109
  identifier: 9781282287105
  identifier: 9786612287107
  identifier: 6612287101
  identifier: 0080923100
  identifier: 9780080923109
  identifier: http://proxy.library.tamu.edu/login
  record info:
    record content source: E7B
    record creation date: 080721
    record change date: 20260326182633.6
    record identifier: in00005745020
    language of cataloging:
      language term: eng